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BCNF is a membership driven organization, which empowers individuals with NF and their families to reach their full potential by providing support, education and research funding.
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Presents the personal aspects of living with the disease, including news, photographs and videos.
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On-line discussion group for people with neurofibromatosis 2.
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Information page compiled by NINDS, the National Institute of Neurological Disorders and Stroke.
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Support group for people with neurofibromatosis. Has a medical and scientific advisory board and close affiliation with similar NF groups overseas.
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Information about neurofibromatosis and details of the center which provides diagnosis, treatment, patient education, and relevant research.
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A non-profit organization for people with NF and their families.
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Photos of cafe au lait spots and external neurofibroma tumors.
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A review of the most important aspects on physical examination, classification and treatment, for medical students.
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Support and information for those with Neurofibromatosis.
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Drug therapies for the treatment of two genetic disorders: neurofibromatosis type 1 (NF1) and neurofibromatosis type 2 (NF2). Find overviews, clinical trials and news.
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Dedicated to promoting awareness of Neurofibromatosis. It also contains the latest research as well as fund raising programs (Marathons, racing, walking, etc) that raise money towards NF research.
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Includes a list of events, fundraisers and outreach programs, as well as background information on the disease, and links to related resources.
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Dedicated to improving the health and well being of individuals and families affected by the neurofibromatosis (NF).
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Information sponsored by the National Neurofibromatosis Foundation for people with NF, and links.
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Information about the UK Association, including family support, membership details and local group contacts.
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This information will explain what NF is, what causes NF, what your family will need to do about it, and who can help you. From the University of Chicago Comer Children's Hospital.
